A clinical trial to compare the effect of a non invasive breathing support modality, high flow nasal cannula against conventional oxygen delivery equipments in preventing patients going back to ventilator after taking them off from it.
Not Applicable
- Conditions
- Health Condition 1: J219- Acute bronchiolitis, unspecifiedHealth Condition 2: G049- Encephalitis, myelitis and encephalomyelitis, unspecifiedHealth Condition 3: Q208- Other congenital malformations ofcardiac chambers and connectionsHealth Condition 4: I518- Other ill-defined heart diseasesHealth Condition 5: D618- Other specified aplastic anemias and other bone marrow failure syndromes
- Registration Number
- CTRI/2021/09/036985
- Lead Sponsor
- arayana Hrudalaya Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients in PICU who will undergo extubation after more than 12 hours of mechanical ventilation.
Exclusion Criteria
Caregivers of patients not giving consent for participating in the study.
Randomization not done due to physician choice of post extubation support.
Diaphragmatic paralysis.
Presence of a tracheostomy tube.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method